Real-World Impact
We recently partnered with a mid-sized pharma SME facing slow patient accrual and ballooning costs. Within weeks:
- Patient recruitment timelines decreased by 25% thanks to predictive enrolment models.
- Site activation issues dropped by 40% due to real-time monitoring.
- Budget variances shrank by 30% with AI-driven resource allocation.
No more chasing outdated reports. No more last-minute protocol amendments lurking in forgotten folders.
Practical Tips for Clinical Trial Optimization
Whether you’re running a Phase I safety study or a global Phase III registration trial, these actionable steps will help you leverage real-time insights:
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Define Your KPIs Upfront
Decide which metrics matter most. Recruitment rate? Adverse event frequency? Protocol deviations? Set thresholds early. -
Automate Data Feeds
Link your eCRF, IVRS/IWRS and lab systems. The less manual handling, the quicker you’ll spot issues. -
Embrace Predictive Models
Use AI to forecast bottlenecks. A sudden dip in enrolment? Address underperforming sites before it’s too late. -
Schedule Weekly Reviews
Even with live data, a human touch is crucial. Meet weekly to review alerts and adjust your plan. -
Iterate Constantly
Feedback fuels improvement. Update algorithms as you learn from each study phase.
Getting Started with Smart Launch
Ready to see Clinical Trial Optimization in action? Here’s how you can begin:
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Start a Free Trial
Test key features on your upcoming study. -
Explore Our Features
Schedule a personalised demo to dive deep into dashboards and analytics. -
Get a Personalised Pilot
Work with our clinical data scientists to tailor Smart Launch to your protocol.
Curious? Your next trial deserves precision, speed and confidence.
Get started with Smart Launch today: https://www.conformancex.com/
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